Canonical Allele Identifier: PA2827005474
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Tyr1633Cys
CA394314314
NM_001318827.2:c.4898A>G